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杀伤细胞免疫球蛋白样受体 2DL4 不能介导 NK 细胞对可溶性 HLA-G 制剂的 IFN-γ 反应。

Killer Ig-like receptor 2DL4 does not mediate NK cell IFN-γ responses to soluble HLA-G preparations.

机构信息

Department of Clinical Immunology, Royal Perth Hospital, Perth, Western Australia 6000, Australia;

出版信息

J Immunol. 2014 Jan 15;192(2):732-40. doi: 10.4049/jimmunol.1301748. Epub 2013 Dec 11.

Abstract

The MHC class Ib molecule HLA-G has previously been reported to be the ligand for the NK cell receptor killer Ig-like receptor (KIR)2DL4, but this remains controversial. In this study, we investigated IFN-γ production by freshly isolated NK cells in response to both soluble and solid-phase ligands, including anti-KIR2DL4 mAbs and rHLA-G. Although freshly isolated CD56(bright) NK cells produced IFN-γ in response to soluble HLA-G preparations, the response was found to be absolutely dependent on the presence of small numbers of contaminating CD56(-), CD14(-), CD11c(+) myeloid dendritic cells (mDCs). HLA-G tetramers bound only to the contaminating mDCs in the NK preparations, and Abs to KIR2DL4 and HLA-G did not block NK cell IFN-γ production. NK cells did not respond to plate-bound HLA-G. Freshly isolated NK cells also produced IFN-γ in response to unpurified soluble anti-KIR2DL4 mAb but not to low endotoxin affinity-purified Ab. The data suggest that previous reports of functional interactions between KIR2DL4 and HLA-G may have resulted from the use of purified NK cells that were contaminated with mDCs and HLA-G preparations that were contaminated with material capable of stimulating mDCs to produce cytokines that stimulate NK cells to produce IFN-γ.

摘要

MHC 类 Ib 分子 HLA-G 先前被报道为 NK 细胞受体杀伤免疫球蛋白样受体(KIR)2DL4 的配体,但这仍然存在争议。在这项研究中,我们研究了新鲜分离的 NK 细胞对可溶性和固相配体(包括抗 KIR2DL4 mAb 和 rHLA-G)产生 IFN-γ 的情况。虽然新鲜分离的 CD56(bright) NK 细胞对可溶性 HLA-G 制剂产生 IFN-γ 的反应,但发现该反应绝对依赖于少量污染的 CD56(-)、CD14(-)、CD11c(+)髓样树突状细胞(mDCs)的存在。HLA-G 四聚体仅与 NK 制剂中污染的 mDC 结合,而 KIR2DL4 和 HLA-G 的 Abs 不能阻断 NK 细胞 IFN-γ 的产生。NK 细胞对板结合的 HLA-G 没有反应。新鲜分离的 NK 细胞也对未纯化的可溶性抗 KIR2DL4 mAb 产生 IFN-γ 的反应,但对低内毒素亲和纯化的 Ab 没有反应。数据表明,先前报道的 KIR2DL4 和 HLA-G 之间的功能相互作用可能是由于使用了污染有 mDCs 和 HLA-G 制剂的纯化 NK 细胞,这些制剂污染有能够刺激 mDCs 产生细胞因子的物质,从而刺激 NK 细胞产生 IFN-γ。

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